Novelli Giuseppe, Spitalieri Paola, Murdocca Michela, Centanini Eleonora, Sangiuolo Federica
Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
IRCCS Neuromed, Pozzilli, IS, Italy.
Front Cell Dev Biol. 2023 Jan 9;10:1059579. doi: 10.3389/fcell.2022.1059579. eCollection 2022.
During the last decades, hiPSC-derived organoids have been extensively studied and used as models for several applications among which research studies. They can be considered as organ and tissue prototypes, especially for those difficult to obtain. Moreover, several diseases can be accurately modeled and studied. Hence, patient-derived organoids (PDOs) can be used to predict individual drug responses, thus paving the way toward personalized medicine. Lastly, by applying tissue engineering and 3D printing techniques, organoids could be used in the future to replace or regenerate damaged tissue. In this review, we will focus on hiPSC-derived 3D cultures and their ability to model human diseases with an in-depth analysis of gene editing applications, as well as tumor models. Furthermore, we will highlight the state-of-the-art of organoid facilities that around the world offer know-how and services. This is an increasing trend that shed the light on the need of bridging the publicand the private sector. Hence, in the context of drug discovery, Organoid Factories can offer biobanks of validated 3D organoid models that can be used in collaboration with pharmaceutical companies to speed up the drug screening process. Finally, we will discuss the limitations and the future development that will lead hiPSC-derived technology from bench to bedside, toward personalized medicine, such as maturity, organoid interconnections, costs, reproducibility and standardization, and ethics. hiPSC-derived organoid technology is now passing from a proof-of-principle to real applications in the clinic, also thanks to the applicability of techniques, such as CRISPR/Cas9 genome editing system, material engineering for the scaffolds, or microfluidic systems. The benefits will have a crucial role in the advance of both basic biological and translational research, particularly in the pharmacological field and drug development. In fact, in the near future, 3D organoids will guide the clinical decision-making process, having validated patient-specific drug screening platforms. This is particularly important in the context of rare genetic diseases or when testing cancer treatments that could in principle have severe side effects. Therefore, this technology has enabled the advancement of personalized medicine in a way never seen before.
在过去几十年里,人诱导多能干细胞(hiPSC)衍生的类器官得到了广泛研究,并被用作多种应用的模型,其中包括研究性研究。它们可被视为器官和组织的原型,尤其是对于那些难以获取的器官和组织。此外,多种疾病能够被精确建模和研究。因此,患者来源的类器官(PDO)可用于预测个体药物反应,从而为个性化医疗铺平道路。最后,通过应用组织工程和3D打印技术,类器官未来可用于替代或再生受损组织。在本综述中,我们将聚焦于hiPSC衍生的3D培养物及其模拟人类疾病的能力,深入分析基因编辑应用以及肿瘤模型。此外,我们将突出世界各地提供专业知识和服务的类器官设施的最新进展。这是一个日益增长的趋势,凸显了弥合公共和私营部门之间差距的必要性。因此,在药物发现的背景下,类器官工厂可以提供经过验证的3D类器官模型生物样本库,可与制药公司合作使用,以加速药物筛选过程。最后,我们将讨论限制因素以及未来的发展方向,这些发展将把hiPSC衍生技术从实验室带到临床床边,迈向个性化医疗,例如成熟度、类器官互连、成本、可重复性和标准化以及伦理问题。hiPSC衍生的类器官技术目前正从原理验证阶段迈向临床实际应用,这也要归功于诸如CRISPR/Cas9基因组编辑系统、支架材料工程或微流控系统等技术的适用性。这些益处将在基础生物学研究和转化研究的推进中发挥关键作用,尤其是在药理学领域和药物开发方面。事实上,在不久的将来,3D类器官将凭借经过验证的患者特异性药物筛选平台指导临床决策过程。这在罕见遗传病的背景下或测试可能具有严重副作用的癌症治疗方法时尤为重要。因此,这项技术以前所未有的方式推动了个性化医疗的发展。